Caesium iodide as an efficient catalyst for synthesis of N-substituted azepines via tandem Michael addition and cyclisation under aqueous conditions

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Abstract

A one-pot synthesis of N-substituted azepines under aqueous conditions is described. The synthesis of several azepines derivatives was carried out by reaction of 2,5-dimethoxytetrahydrofuran, aromatic amines and dimethyl/diethyl acetylene dicarboxylate in the presence of CsI in water at ambient temperature. Products were obtained in high yields and catalyst was recovered and reused without a significant decrease in catalytic activity.

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Eshghi, H., Momen, S., Gholizadeh, M., & Vakili, M. (2013). Caesium iodide as an efficient catalyst for synthesis of N-substituted azepines via tandem Michael addition and cyclisation under aqueous conditions. Journal of Chemical Research, 37(12), 724–726. https://doi.org/10.3184/174751913X13824449342828

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